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Somatic mutations in benign breast disease tissues and association with breast cancer risk.
Winham SJ, Wang C, Heinzen EP, Bhagwate A, Liu Y, McDonough SJ, Stallings-Mann ML, Frost MH, Vierkant RA, Denison LA, Carter JM, Sherman ME, Radisky DC, Degnim AC, Cunningham JM. Winham SJ, et al. Among authors: bhagwate a. BMC Med Genomics. 2021 Jul 14;14(1):185. doi: 10.1186/s12920-021-01032-8. BMC Med Genomics. 2021. PMID: 34261476 Free PMC article.
Quality control recommendations for RNASeq using FFPE samples based on pre-sequencing lab metrics and post-sequencing bioinformatics metrics.
Liu Y, Bhagwate A, Winham SJ, Stephens MT, Harker BW, McDonough SJ, Stallings-Mann ML, Heinzen EP, Vierkant RA, Hoskin TL, Frost MH, Carter JM, Pfrender ME, Littlepage L, Radisky DC, Cunningham JM, Degnim AC, Wang C. Liu Y, et al. Among authors: bhagwate a. BMC Med Genomics. 2022 Sep 16;15(1):195. doi: 10.1186/s12920-022-01355-0. BMC Med Genomics. 2022. PMID: 36114500 Free PMC article.
Gene expression, single nucleotide variant and fusion transcript discovery in archival material from breast tumors.
Norton N, Sun Z, Asmann YW, Serie DJ, Necela BM, Bhagwate A, Jen J, Eckloff BW, Kalari KR, Thompson KJ, Carr JM, Kachergus JM, Geiger XJ, Perez EA, Thompson EA. Norton N, et al. Among authors: bhagwate a. PLoS One. 2013 Nov 22;8(11):e81925. doi: 10.1371/journal.pone.0081925. eCollection 2013. PLoS One. 2013. PMID: 24278466 Free PMC article.
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.
Wang C, Evans JM, Bhagwate AV, Prodduturi N, Sarangi V, Middha M, Sicotte H, Vedell PT, Hart SN, Oliver GR, Kocher JP, Maurer MJ, Novak AJ, Slager SL, Cerhan JR, Asmann YW. Wang C, et al. Among authors: bhagwate av. Bioinformatics. 2014 Sep 15;30(18):2678-80. doi: 10.1093/bioinformatics/btu363. Epub 2014 May 29. Bioinformatics. 2014. PMID: 24876377 Free PMC article.
37 results